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Primary ciliary dyskinesia: age at diagnosis and symptom history.
Coren ME, Meeks M, Morrison I, Buchdahl RM, Bush A. Coren ME, et al. Among authors: meeks m. Acta Paediatr. 2002;91(6):667-9. doi: 10.1080/080352502760069089. Acta Paediatr. 2002. PMID: 12162599
Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia.
Bartoloni L, Blouin JL, Maiti AK, Sainsbury A, Rossier C, Gehrig C, She JX, Marron MP, Lander ES, Meeks M, Chung E, Armengot M, Jorissen M, Scott HS, Delozier-Blanchet CD, Gardiner RM, Antonarakis SE. Bartoloni L, et al. Among authors: meeks m. Genomics. 2001 Feb 15;72(1):21-33. doi: 10.1006/geno.2000.6462. Genomics. 2001. PMID: 11247663
No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD).
Maiti AK, Bartoloni L, Mitchison HM, Meeks M, Chung E, Spiden S, Gehrig C, Rossier C, DeLozier-Blanchet CD, Blouin J, Gardiner RM, Antonarakis SE. Maiti AK, et al. Among authors: meeks m. Cytogenet Cell Genet. 2000;90(1-2):119-22. doi: 10.1159/000015645. Cytogenet Cell Genet. 2000. PMID: 11060460
Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity.
Blouin JL, Meeks M, Radhakrishna U, Sainsbury A, Gehring C, Saïl GD, Bartoloni L, Dombi V, O'Rawe A, Walne A, Chung E, Afzelius BA, Armengot M, Jorissen M, Schidlow DV, van Maldergem L, Walt H, Gardiner RM, Probst D, Guerne PA, Delozier-Blanchet CD, Antonarakis SE. Blouin JL, et al. Among authors: meeks m. Eur J Hum Genet. 2000 Feb;8(2):109-18. doi: 10.1038/sj.ejhg.5200429. Eur J Hum Genet. 2000. PMID: 10757642
Primary ciliary dyskinesia (PCD).
Meeks M, Bush A. Meeks M, et al. Pediatr Pulmonol. 2000 Apr;29(4):307-16. doi: 10.1002/(sici)1099-0496(200004)29:4<307::aid-ppul11>3.0.co;2-2. Pediatr Pulmonol. 2000. PMID: 10738019 Review.
A locus for primary ciliary dyskinesia maps to chromosome 19q.
Meeks M, Walne A, Spiden S, Simpson H, Mussaffi-Georgy H, Hamam HD, Fehaid EL, Cheehab M, Al-Dabbagh M, Polak-Charcon S, Blau H, O'Rawe A, Mitchison HM, Gardiner RM, Chung E. Meeks M, et al. J Med Genet. 2000 Apr;37(4):241-4. doi: 10.1136/jmg.37.4.241. J Med Genet. 2000. PMID: 10745040 Free PMC article.
Cilia, primary ciliary dyskinesia and molecular genetics.
Chodhari R, Mitchison HM, Meeks M. Chodhari R, et al. Among authors: meeks m. Paediatr Respir Rev. 2004 Mar;5(1):69-76. doi: 10.1016/j.prrv.2003.09.005. Paediatr Respir Rev. 2004. PMID: 15222957 Review.
Loci for primary ciliary dyskinesia map to chromosome 16p12.1-12.2 and 15q13.1-15.1 in Faroe Islands and Israeli Druze genetic isolates.
Jeganathan D, Chodhari R, Meeks M, Faeroe O, Smyth D, Nielsen K, Amirav I, Luder AS, Bisgaard H, Gardiner RM, Chung EM, Mitchison HM. Jeganathan D, et al. Among authors: meeks m. J Med Genet. 2004 Mar;41(3):233-40. doi: 10.1136/jmg.2003.014084. J Med Genet. 2004. PMID: 14985390 Free PMC article. No abstract available.
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry.
Olbrich H, Häffner K, Kispert A, Völkel A, Volz A, Sasmaz G, Reinhardt R, Hennig S, Lehrach H, Konietzko N, Zariwala M, Noone PG, Knowles M, Mitchison HM, Meeks M, Chung EM, Hildebrandt F, Sudbrak R, Omran H. Olbrich H, et al. Among authors: meeks m. Nat Genet. 2002 Feb;30(2):143-4. doi: 10.1038/ng817. Epub 2002 Jan 14. Nat Genet. 2002. PMID: 11788826
PCD or not PCD.
Meeks M, Coren M. Meeks M, et al. Arch Dis Child. 2003 May;88(5):460. doi: 10.1136/adc.88.5.460-a. Arch Dis Child. 2003. PMID: 12716729 Free PMC article. No abstract available.
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